FUNGAL NAIL TREATMENT kit .cream.

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: FUNGAL NAIL TREATMENT kit .cream.
Generic name: PSEUDOLARIX AMABILIS BARK 1%
Manufacturer: GETHSEMANE BRANCH CORPORATION
Product type: HUMAN OTC DRUG
SPL set ID: 56c9d9fa-09ad-e26a-e063-6394a90a0ed9
SPL ID: 56c9d9fa-09ae-e26a-e063-6394a90a0ed9
Version: 1
Effective date: 2026-07-17
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:41

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		FUNGAL NAIL TREATMENT kit .cream.	openfda.brand_name
generic name		PSEUDOLARIX AMABILIS BARK 1%	openfda.generic_name
manufacturer name		GETHSEMANE BRANCH CORPORATION	openfda.manufacturer_name
ndc	package	87870-002-01	openfda.package_ndc
ndc	product	87870-002	openfda.product_ndc
ndc11	package	87870000201	derived:openfda.package_ndc
spl id		56c9d9fa-09ae-e26a-e063-6394a90a0ed9	id
spl set id		56c9d9fa-09ad-e26a-e063-6394a90a0ed9	set_id
unii		6DC9Q167V3	openfda.unii
unii		49G13A93VE	openfda.unii
unii		CXS4LJR7EL	openfda.unii
unii		O414PZ4LPZ	openfda.unii
unii		M89NIB437X	openfda.unii
unii		CAZ6282J2O	openfda.unii
unii		N20HL7Q941	openfda.unii
unii		IYR6K8KQ5K	openfda.unii
unii		FXG254HF10	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

For external use only. Do not use on irritated skin on any area that is infected or reddened Do not use it if pregnant or if there is any allergic reaction to this product Avoid contact with eyes. Ask a doctor before you use If you have diabetes or poor blood circulation Stop use and ask a doctor If discomfort persists If product gets into eyes, flush with water for 15 minutes If swallowed, get medical help or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.